Qualified Person (QP) - Sterile Manufacturing
Are you a Qualified Person with experience in sterile pharmaceutical manufacturing? Looking to make an impact in a forward-thinking company where quality and patient safety come first?
Smart4 Sciences are working with a pharmaceutical manufacturer in Essex specialising in the production of sterile and non-sterile products. As part of their continued expansion, they're seeking an experienced and proactive Qualified Person to join their quality team.
The Role:
As a QP, you'll be responsible for ensuring that products released to market meet the highest standards of GMP compliance and patient safety. Working in a modern GMP facility, you will:
Act as a QP for the certification and release of sterile pharmaceutical products
Ensure full compliance with MHRA and EU GMP guidelines
Liaise closely with QA, Production, and Regulatory Affairs teams
Contribute to audits, inspections, and continuous improvement projects
Support the development of junior QA staff and provide QP oversight where needed
About You:
Eligible to act as a Qualified Person under Directive 2001/83/EC
Prior experience working with sterile manufacturing (aseptic/terminally sterilised products) is desirable
Strong working knowledge of EU GMP and UK pharmaceutical regulations
If you're a QP ready for your next challenge in a state-of-the-art sterile manufacturing environment, we'd love to hear from you!
Apply today or contact Gareth Gooley on for a confidential discussion